Long non-coding RNA (lncRNA) HOXD-AS2 promotes glioblastoma cell proliferation, migration and invasion by regulating the miR-3681-5p/MALT1 signaling pathway

Glioblastoma (GBM) is the most lethal type of brain cancer. An increasing number of studies suggest that long non-coding RNAs (lncRNAs) are implicated in tumor progression. LncRNA HOXD‐AS2 was reported to be highly expressed in glioma and associated with glioma grade and poor prognosis. However, the...

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Autores principales: Xingming Zhong, Yong Cai
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Publicado: Taylor & Francis Group 2021
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Acceso en línea:https://doaj.org/article/800a3d89436a4072bf6f5748517dc50e
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spelling oai:doaj.org-article:800a3d89436a4072bf6f5748517dc50e2021-11-26T11:19:49ZLong non-coding RNA (lncRNA) HOXD-AS2 promotes glioblastoma cell proliferation, migration and invasion by regulating the miR-3681-5p/MALT1 signaling pathway2165-59792165-598710.1080/21655979.2021.1977104https://doaj.org/article/800a3d89436a4072bf6f5748517dc50e2021-12-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.1977104https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987Glioblastoma (GBM) is the most lethal type of brain cancer. An increasing number of studies suggest that long non-coding RNAs (lncRNAs) are implicated in tumor progression. LncRNA HOXD‐AS2 was reported to be highly expressed in glioma and associated with glioma grade and poor prognosis. However, the molecular mechanism remains to be elucidated. In this study, we first analyzed differentially expressed lncRNAs in glioblastoma using RNA-seq dataset (156 GBM samples and 5 adjacent normal samples in TCGA (Cancer Genome Atlas) and GTEx (Genotype-Tissue Expression) database). HOXD-AS2 was found to be significantly up-regulated in GBM tissues, which was further confirmed in GBM patient tumor samples and GBM cell lines. Silencing HOXD-AS2 inhibited cell proliferation, migration and invasion, and promoted cell apoptosis. We further identified and validated miR-3681-5p as a target of HOXD-AS2, and miR-3681-5p was negatively regulated by HOXD-AS2. By negatively affecting miR-3681-5p, HOXD-AS2 could promote the expression of MALT1 to augment the aggressiveness of GBM cells. miR-3681-5p overexpression or MALT1 knockdown attenuated aggressiveness of GBM cells. Importantly, silencing HOXD-AS2 suppressed tumorigenesis of GBM cells in the xenograft mouse model. Collectively, our study clarified the role of miR-3681-5p/MALT1 axis underlying the oncogenic function of lncRNA HOXD-AS2 in GBM. Future work is required to study the mechanism by which HOXD-AS2 is upregulated in GBM cells, which can provide novel insights into therapeutic intervention for GBM treatment.Xingming ZhongYong CaiTaylor & Francis Grouparticleglioblastomalncrna hoxd‐as2mir-3681-5pmalt1BiotechnologyTP248.13-248.65ENBioengineered, Vol 12, Iss 2, Pp 9113-9127 (2021)
institution DOAJ
collection DOAJ
language EN
topic glioblastoma
lncrna hoxd‐as2
mir-3681-5p
malt1
Biotechnology
TP248.13-248.65
spellingShingle glioblastoma
lncrna hoxd‐as2
mir-3681-5p
malt1
Biotechnology
TP248.13-248.65
Xingming Zhong
Yong Cai
Long non-coding RNA (lncRNA) HOXD-AS2 promotes glioblastoma cell proliferation, migration and invasion by regulating the miR-3681-5p/MALT1 signaling pathway
description Glioblastoma (GBM) is the most lethal type of brain cancer. An increasing number of studies suggest that long non-coding RNAs (lncRNAs) are implicated in tumor progression. LncRNA HOXD‐AS2 was reported to be highly expressed in glioma and associated with glioma grade and poor prognosis. However, the molecular mechanism remains to be elucidated. In this study, we first analyzed differentially expressed lncRNAs in glioblastoma using RNA-seq dataset (156 GBM samples and 5 adjacent normal samples in TCGA (Cancer Genome Atlas) and GTEx (Genotype-Tissue Expression) database). HOXD-AS2 was found to be significantly up-regulated in GBM tissues, which was further confirmed in GBM patient tumor samples and GBM cell lines. Silencing HOXD-AS2 inhibited cell proliferation, migration and invasion, and promoted cell apoptosis. We further identified and validated miR-3681-5p as a target of HOXD-AS2, and miR-3681-5p was negatively regulated by HOXD-AS2. By negatively affecting miR-3681-5p, HOXD-AS2 could promote the expression of MALT1 to augment the aggressiveness of GBM cells. miR-3681-5p overexpression or MALT1 knockdown attenuated aggressiveness of GBM cells. Importantly, silencing HOXD-AS2 suppressed tumorigenesis of GBM cells in the xenograft mouse model. Collectively, our study clarified the role of miR-3681-5p/MALT1 axis underlying the oncogenic function of lncRNA HOXD-AS2 in GBM. Future work is required to study the mechanism by which HOXD-AS2 is upregulated in GBM cells, which can provide novel insights into therapeutic intervention for GBM treatment.
format article
author Xingming Zhong
Yong Cai
author_facet Xingming Zhong
Yong Cai
author_sort Xingming Zhong
title Long non-coding RNA (lncRNA) HOXD-AS2 promotes glioblastoma cell proliferation, migration and invasion by regulating the miR-3681-5p/MALT1 signaling pathway
title_short Long non-coding RNA (lncRNA) HOXD-AS2 promotes glioblastoma cell proliferation, migration and invasion by regulating the miR-3681-5p/MALT1 signaling pathway
title_full Long non-coding RNA (lncRNA) HOXD-AS2 promotes glioblastoma cell proliferation, migration and invasion by regulating the miR-3681-5p/MALT1 signaling pathway
title_fullStr Long non-coding RNA (lncRNA) HOXD-AS2 promotes glioblastoma cell proliferation, migration and invasion by regulating the miR-3681-5p/MALT1 signaling pathway
title_full_unstemmed Long non-coding RNA (lncRNA) HOXD-AS2 promotes glioblastoma cell proliferation, migration and invasion by regulating the miR-3681-5p/MALT1 signaling pathway
title_sort long non-coding rna (lncrna) hoxd-as2 promotes glioblastoma cell proliferation, migration and invasion by regulating the mir-3681-5p/malt1 signaling pathway
publisher Taylor & Francis Group
publishDate 2021
url https://doaj.org/article/800a3d89436a4072bf6f5748517dc50e
work_keys_str_mv AT xingmingzhong longnoncodingrnalncrnahoxdas2promotesglioblastomacellproliferationmigrationandinvasionbyregulatingthemir36815pmalt1signalingpathway
AT yongcai longnoncodingrnalncrnahoxdas2promotesglioblastomacellproliferationmigrationandinvasionbyregulatingthemir36815pmalt1signalingpathway
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